NDC 16103-382 - Ferrous Sulfate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 16103-382
- Package NDCs from labels
- 16103-382-08, 16103-382-11
- Manufacturer
- Pharbest Pharmaceuticals, Inc.
- Effective date
- 2019-07-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ferrous Sulfate - Pharbest Pharmaceuticals, Inc. | Pharbest Pharmaceuticals, Inc. | 2019-07-23 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16103-382-08 | Ferrous Sulfate | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 1 | |
| 16103-382-11 | Ferrous Sulfate | 1000 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1000 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16103-382-08 | EA - Each | 16103-382 | 89b098e8-9d6f-4fe4-bfd1-5b2e49c1466a | 1 | 2021-04-08 |
| 16103-382-11 | EA - Each | 16103-382 | 65f33516-e3cd-45a4-aaec-a5c7e1630c93 | 1 | 2021-04-08 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.